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MMP 9 ELISA Kit (Matrix Metallopeptidase 9 (Gelatinase B, 92kDa Gelatinase, 92kDa Type IV Collagenase)) ELISA Kit

MMP9 Reactivity: Mouse Colorimetric Sandwich ELISA 0.15 ng/mL - 10 ng/mL Cell Culture Supernatant, Cell Lysate, Plasma, Serum, Tissue Homogenate
Pubmed (10 references)
Catalog No. ABIN6730931
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  • Target See all MMP 9 (MMP9) ELISA Kits
    MMP 9 (MMP9)
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    Detection Method
    Method Type
    Sandwich ELISA
    Detection Range
    0.15 ng/mL - 10 ng/mL
    Minimum Detection Limit
    0.15 ng/mL
    The kit is a sandwich enzyme immunoassay for in vitro quantitative measurement of MMP9 in mouse serum, plasma, tissue homogenates, cell lysates, cell culture supernates.

    We offer validation data (WB) for the kit components. So you can be sure to order a reliable ELISA kit product composed of high quality reagents.
    Sample Type
    Cell Culture Supernatant, Cell Lysate, Plasma, Serum, Tissue Homogenate
    Analytical Method
    This assay has high sensitivity and excellent specificity for detection of Matrix Metalloproteinase 9 (MMP9)
    Cross-Reactivity (Details)
    No significant cross-reactivity or interference between Matrix Metalloproteinase 9 (MMP9) and analogues was observed.
    0.057 ng/mL
    • Pre-coated, ready to use 96-well strip plate, flat buttom
    • Plate sealer for 96 wells
    • Reference Standard
    • Standard Diluent
    • Detection Reagent A
    • Detection Reagent B
    • Assay Diluent A
    • Assay Diluent B
    • Reagent Diluent (if Detection Reagent is lyophilized)
    • TMB Substrate
    • Stop Solution
    • Wash Buffer (30 x concentrate)
    • Instruction manual
  • Comment

    Information on standard material:
    The standard might be recombinant protein or natural protein, that will depend on the specific kit. Moreover, the expression system is E.coli or yeast or mammal cell. There is 0.05% proclin 300 in the standard as preservative.

    Information on reagents:
    The stop solution used in the kit is sulfuric acid with concentration of 1 mol/L. And the wash solution is TBS. The standard diluent contains 0.02 % sodium azide, assay diluent A and assay diluent B contain 0.01% sodium azide. Some kits can contain is BSA in them.

    Information on antibodies:
    The provided antibodies and their host vary in different kits.

    Sample Volume
    100 μL
    Assay Time
    3 h
    1. Prepare all reagents, samples and standards,
    2. Add 100μL standard or sample to each well. Incubate 1 hours at 37 °C,
    3. Aspirate and add 100μL prepared Detection Reagent A. Incubate 1 hour at 37 °C,
    4. Aspirate and wash 3 times,
    5. Add 100μL prepared Detection Reagent B. Incubate 30 minutes at 37 °C,
    6. Aspirate and wash 5 times,
    7. Add 90μL Substrate Solution. Incubate 10-20 minutes at 37 °C,
    8. Add 50μL Stop Solution. Read at 450nm immediately.
    Reagent Preparation
    1. Bring all kit components and samples to room temperature (18-25 °C) before use. If the kit will not be used up in one time, please only take out strips and reagents for present experiment, and leave the remaining strips and reagents in required condition.
    2. Standard - Reconstitute the Standard with 1.0 mL of Standard Diluent, keep for 10 minutes at room temperature, shake gently (not to foam). The concentration of the standard in the stock solution is 40 ng/mL. Firstly dilute the stock solution to 10 ng/mL and the diluted standard serves as the highest standard (10 ng/mL). Then prepare 7 tubes containing 0.5 mL Standard Diluent and use the diluted standard to produce a double dilution series. Mix each tube thoroughly before the next transfer. Set up 7 points of diluted standard such as 10 ng/mL, 5 ng/mL, 2.5 ng/mL, 1.25 ng/mL, 0.625 ng/mL, 0.312 ng/mL, 0.156 ng/mL, and the last microcentrifuge tube with Standard Diluent is the blank as 0 ng/mL.
    3. Detection Reagent A and Detection Reagent B - If lyophilized reconstitute the Detection Reagent A with 150μL of Reagent Diluent, keep for 10 minutes at room temperature, shake gently (not to foam). Briefly spin or centrifuge the stock Detection A and Detection B before use. Dilute them to the working concentration 100-fold with Assay Diluent A and B, respectively.
    4. Wash Solution - Dilute 20 mL of Wash Solution concentrate (30x) with 580 mL of deionized or distilled water to prepare 600 mL of Wash Solution (1x).
    5. TMB substrate - Aspirate the needed dosage of the solution with sterilized tips and do not dump the residual solution into the vial again.


    1. Making serial dilution in the wells directly is not permitted.
    2. Prepare standards within 15 minutes before assay. Please do not dissolve the reagents at 37 °C directly.
    3. Please carefully reconstitute Standards or working Detection Reagent A and B according to the instruction, and avoid foaming and mix gently until the crystals are completely dissolved. To minimize imprecision caused by pipetting, use small volumes and ensure that pipettors are calibrated. It is recommended to suck more than 10μL for one pipetting.
    4. The reconstituted Standards, Detection Reagent A and Detection Reagent B can be used only once.
    5. If crystals have formed in the Wash Solution concentrate (30x), warm to room temperature and mix gently until the crystals are completely dissolved.
    6. Contaminated water or container for reagent preparation will influence the detection result.
    Sample Preparation
    • It is recommended to use fresh samples without long storage, otherwise protein degradation and denaturationmay occur in these samples, leading to false results. Samples should therefore be stored for a short periodat 2 - 8 °C or aliquoted at -20 °C (≤1 month) or -80 °C (≤ 3 months). Repeated freeze-thawcycles should be avoided. Prior to assay, the frozen samples should be slowly thawed and centrifuged toremove precipitates.
    • If the sample type is not specified in the instructions, a preliminary test is necessary to determinecompatibility with the kit.
    • If a lysis buffer is used to prepare tissue homogenates or cell culture supernatant, there is a possibilityof causing a deviation due to the introduced chemical substance.The recommended dilution factor is for reference only.
    • Please estimate the concentration of the samples before performing the test. If the values are not in therange of the standard curve, the optimal sample dilution for the particular experiment has to be determined.Samples should then be diluted with PBS (pH =7.0-7.2).
    Assay Precision
    Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level of target were tested 20 times on one plate, respectively.
    Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level of target were tested on 3 different plates, 8 replicates in each plate.
    CV(%) = SD/meanX100
    Intra-Assay: CV < 10%
    Inter-Assay: CV < 12%
    For Research Use only
  • Precaution of Use
    The Stop Solution suggested for use with this kit is an acid solution. Wear eye, hand, face, and clothing protection when using this material.
    4 °C/-20 °C
    Storage Comment
    1. For unopened kit: All reagents should be stored according to the labels on the vials. The Standard, Detection Reagent A, Detection Reagent B, and 96-well Strip Plate should be stored at -20 °C upon receipt, while the other reagents should be stored at 4 °C.
    2. For opened kits: the remaining reagents must be stored according to the above storage conditions. In addition, please return the unused wells to the foil pouch containing the desiccant and seal the foil pouch with the zipper.
    Expiry Date
    6 months
  • Taverna, Pucci, Giallombardo, Di Bella, Santarpia, Reclusa, Gil-Bazo, Rolfo, Alessandro: "Amphiregulin contained in NSCLC-exosomes induces osteoclast differentiation through the activation of EGFR pathway." in: Scientific reports, Vol. 7, Issue 1, pp. 3170, (2018) (PubMed).

    Lin, Chou, Chiang, Chen: "CTGF upregulation correlates with MMP-9 level in airway remodeling in a murine model of asthma." in: Archives of medical science : AMS, Vol. 13, Issue 3, pp. 670-676, (2017) (PubMed).

    Yoshizaki, Brito, Silva, Lino-Dos-Santos-Franco, Frias, E Silva, Amato-Lourenço, Saldiva, de Fátima Lopes Calvo Tibério, Mauad, Macchione: "The effects of particulate matter on inflammation of respiratory system: Differences between male and female." in: The Science of the total environment, Vol. 586, pp. 284-295, (2017) (PubMed).

    Suh, Chon, Choi: "Actein protects against methylglyoxal-induced oxidative damage in osteoblastic MC3T3-E1 cells." in: Journal of the science of food and agriculture, (2016) (PubMed).

    Muhammad, Planz, Schwaninger: "Increased Plasma Matrix Metalloproteinase-9 Levels Contribute to Intracerebral Hemorrhage during Thrombolysis after Concomitant Stroke and Influenza Infection." in: Cerebrovascular diseases extra, Vol. 6, Issue 2, pp. 50-9, (2016) (PubMed).

    Gao, Guo, Zeng, Wang, Yang, Pang, Li, Suo, Jiang, Yu: "Matrix metalloproteinase 9 secreted by hypoxia cardiac fibroblasts triggers cardiac stem cell migration in vitro." in: Stem cells international, Vol. 2015, pp. 836390, (2015) (PubMed).

    Hattori, Ishihara: "Altered protein secretions during interactions between adipose tissue- or bone marrow-derived stromal cells and inflammatory cells." in: Stem cell research & therapy, Vol. 6, pp. 70, (2015) (PubMed).

    Yao, Cao, He, Lau, Zeng, Liang: "Adiponectin attenuates lung fibroblasts activation and pulmonary fibrosis induced by paraquat." in: PLoS ONE, Vol. 10, Issue 5, pp. e0125169, (2015) (PubMed).

    Lenglet, Montecucco, Mach, Schaller, Gasche, Copin: "Analysis of the expression of nine secreted matrix metalloproteinases and their endogenous inhibitors in the brain of mice subjected to ischaemic stroke." in: Thrombosis and haemostasis, Vol. 112, Issue 2, pp. 363-78, (2014) (PubMed).

    Chia, Pan, Tseng, Chen, Feng, Lee, Chang, Sytwu: "Experimental osteoarthritis induced by surgical realignment of the patella in BALB/c mice." in: The Journal of bone and joint surgery. British volume, Vol. 92, Issue 12, pp. 1710-6, (2010) (PubMed).

  • Target See all MMP 9 (MMP9) ELISA Kits
    MMP 9 (MMP9)
    Alternative Name
    Matrix Metalloproteinase 9 (MMP9) (MMP9 Products)
    CLG4B, GELB, MANDP2, MMP-9, AW743869, B/MMP9, Clg4b, pro-MMP-9, mmp-9, fgMMP-9, mmp9, ZFMMP-9, wu:fb02g06, wu:fb07b05, wu:fi98c09, wu:fj05a08, zgc:64165, clg4b, gelb, mandp2, matrix metallopeptidase 9, collagenase, matrix metalloproteinase 9, matrix metallopeptidase 9 S homeolog, MMP9, RB3913, BPSS0666, Sbal_3732, Bcer98_0486, Shew185_0630, Shal_3056, Sbal195_0657, Lbys_3550, Palpr_2084, Mmp9, mmp9, mmp9.S
    Cellular Response to Molecule of Bacterial Origin, Positive Regulation of Immune Effector Process, CXCR4-mediated Signaling Events
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